Recalls distributed in Hawaii
These notices name Hawaii in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
1,581 stored notices name Hawaii, reported between Jun 27, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Hawaii too — those are in the archive.
Reported Sep 30, 2026Updated Oct 6, 2026
ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The non-invasive ForeSight oximeter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 6, 2026
nGenuity Patient Monitor with Capnography (ETCO2) CAT 8100E1-ST-US, CAT 8100E1-US, CAT 8100EP1, CAT 8100EP1-ST, CAT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Criticare Technologies, Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 7, 2026
Reese's Crunchy Peanut Ice Cream Bar, 2.0 fl. oz. ice cream bars, paper cartons containing individually wrapped ice…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Unilever North America Supply Chain Company, LLC
FDA (weekly enforcement report)
Reported Sep 23, 2026Updated Sep 29, 2026
Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bard Access Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2026Updated Sep 29, 2026
BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bd Switzerland Sarl
FDA (openFDA device enforcement)
Reported Sep 23, 2026Updated Sep 29, 2026
Boston Scientific Corporation StoneSmart Connect Console Contents: (1) Power Cord, (1) Power Adaptor, (1)DVI Cable, (1)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Sep 23, 2026Updated Sep 29, 2026
Happiest Baby, Inc SNOO Sleep Sack, X-Small Model/Catalog Number: S2101-101 S2101-108-6 S2101-133 S2102-112 S2107-101…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Happiest Baby, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2026Updated Sep 29, 2026
Plum administration sets
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2026Updated Sep 29, 2026
Philips Patient Information Center iX REF:866389
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2026Updated Sep 29, 2026
REF:2B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW TECHNOLOGY & SLEEVE 5MM X 75MM
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2026Updated Sep 29, 2026
Brand Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Product Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Model/Catalog Number: HEMO-7,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wilson-Cook Medical Inc.
FDA (openFDA device enforcement)
Reported Sep 16, 2026Updated Sep 22, 2026
Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2026Updated Sep 22, 2026
HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartSine Technologies Ltd.
FDA (openFDA device enforcement)
Reported Sep 16, 2026Updated Sep 22, 2026
Alfalfa, Net Weight 50 lbs. bag, Product of USA, International Specialty Supply 1011 Volunteer Dr. Cookeville, TN 38506
High riskUsing this product could cause serious injury, illness or death — stop using it now.International Sprout Holdings, Inc.
FDA (openFDA food enforcement)
Reported Sep 9, 2026Updated Sep 14, 2026
Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number: 456025
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B Braun Medical Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2026Updated Sep 14, 2026
Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
20 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 9, 2026Updated Sep 14, 2026
HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN) HEALON EndoCoat PRO, REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision, Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2026Updated Sep 16, 2026
Food to Live brand Organic Supergreens mix (kale, moringa leaf, wheat grass, & spirulina), 8 oz, 1 lb, 1.5 lb, 3 lb, 6…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lexunder Inc.
FDA (weekly enforcement report)
Reported Sep 2, 2026Updated Sep 13, 2026
Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Byron White Formulas, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 2, 2026Updated Sep 7, 2026
Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base. Retail package net wt. 15.4oz. Product is ramen…
High riskUsing this product could cause serious injury, illness or death — stop using it now.H & U Inc. dba Sun Noodle
FDA (openFDA food enforcement)
Reported Sep 2, 2026Updated Sep 7, 2026
Glutinous Rice Balls with Black Sesame Filling NET WT. 14.1 OZ (400 g) Product of China UPC: 6908791000053
High riskUsing this product could cause serious injury, illness or death — stop using it now.Khong Guan (hq)
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
Arrow-LOK Implant, REF: 21-253519, 21-253522, 21-253525, 21-253528, 21-253530, 21-253533, 21-253535, 21-253540,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrowhead DE LLC
FDA (openFDA device enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Model/Catalog Number: IN-29200…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kico Knee Innovation Company
FDA (openFDA device enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
Paragonix Technologies Inc. KidneyVault Portable Renal Perfusion System REF# PRGNX-8008-001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paragonix Technologies Inc.
FDA (openFDA device enforcement)
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Other states
RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.